Literature DB >> 16318910

Richner-Hanhart syndrome: report of a case with a novel mutation of tyrosine aminotransferase.

M Minami-Hori, A Ishida-Yamamoto, N Katoh, H Takahashi, H Iizuka.   

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Year:  2005        PMID： 16318910     DOI： 10.1016/j.jdermsci.2005.10.007

Source DB:  PubMed          Journal:  J Dermatol Sci        ISSN： 0923-1811            Impact factor:   4.563


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  3 in total

1.  TAT gene mutation analysis in three Palestinian kindreds with oculocutaneous tyrosinaemia type II; characterization of a silent exonic transversion that causes complete missplicing by exon 11 skipping.

Authors:  G Maydan; B S Andresen; P P Madsen; M Zeigler; A Raas-Rothschild; A Zlotogorski; A Gutman; S H Korman
Journal:  J Inherit Metab Dis       Date:  2006-08-17       Impact factor: 4.982

2.  Tyrosine aminotransferase: biochemical and structural properties and molecular dynamics simulations.

Authors:  Prajwalini Mehere; Qian Han; Justin A Lemkul; Christopher J Vavricka; Howard Robinson; David R Bevan; Jianyong Li
Journal:  Protein Cell       Date:  2010-12-10       Impact factor: 14.870

3.  Relaxed evolution in the tyrosine aminotransferase gene tat in old world fruit bats (Chiroptera: Pteropodidae).

Authors:  Bin Shen; Tao Fang; Tianxiao Yang; Gareth Jones; David M Irwin; Shuyi Zhang
Journal:  PLoS One       Date:  2014-05-13       Impact factor: 3.240
  3 in total

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